Synthesis and evaluation of [11C]cyanoimipramine

Int J Rad Appl Instrum B. 1987;14(6):587-92. doi: 10.1016/0883-2897(87)90030-4.

Abstract

[11C]Cyanoimipramine has been prepared by methylation of the desmethyl cyanoimipramine with [11C]methyl iodide. The chemically and radiochemically pure labelled product was obtained with a high specific activity (greater than 300 mCi/mumol). When 11C (or 3H)-cyanoimipramine was intravenously administered in mice, high accumulations were shown in brain and lung. Thirty minutes after injection of the tracer, differences were found in the radioactivity between the cerebral cortex and the cerebellum. The regional distribution of radioactivity in the rat brain 30 min after i.v. injection of [11C]cyanoimipramine was also examined, and the radioactivity was high in receptor rich areas (striatum, cerebral cortex etc.) but low in receptor poor area (cerebellum). The in vivo stability of [3H]cyanoimipramine was quite stable in the mouse brain for at least 30 min. Thirty minutes after injection, the radioactivity in the cerebral cortex of the carrier-added state was reduced as compared with the carrier-free state. Taken together, the in vivo specific binding of [3H]cyanoimipramine in the cerebral cortex was estimated at about 40-50% of the total radioactivity. Furthermore, the distribution of [3H]cyanoimipramine in the mice forced to swim was examined. Significant changes in the distribution of [3H]cyanoimipramine were observed in the cerebral cortex.

MeSH terms

  • Animals
  • Brain / metabolism
  • Carbon Radioisotopes
  • Imipramine / analogs & derivatives*
  • Imipramine / chemical synthesis
  • Imipramine / pharmacokinetics
  • Kinetics
  • Male
  • Mice
  • Mice, Inbred C3H
  • Serotonin Antagonists / chemical synthesis*
  • Tissue Distribution

Substances

  • Carbon Radioisotopes
  • Serotonin Antagonists
  • cianopramine
  • Imipramine